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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Timmers C, etal., Mol Cell. 2001 Feb;7(2):241-8.
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Timmers C, etal., Mol Cell. 2001 Feb;7(2):241-8.
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: DNA:missense mutations, nonsense mutation, splice-site mutation: :multiple


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Pilonetto DV, etal., Braz J Med Biol Res. 2009 Mar;42(3):237-43.
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IDA) inferred from direct assay]
  • 2 additional annotations were made from Pilonetto DV, etal., Braz J Med Biol Res. 2009 Mar;42(3):237-43.
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(EXP) inferred from experiment]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:14667412


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17096012 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:22829014 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24584348 PMID:24728327 PMID:25640679 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:30716324 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33270637 PMID:33558524 PMID:34327028 PMID:34585473 PMID:36463940 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia | ClinVar Annotator: match by term: Fanconi pancytopenia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24728327 PMID:25640679 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33558524 PMID:34585473 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia
  • Original References(s): PMID:11239453 PMID:16199547 PMID:16280053 PMID:17436244 PMID:17576681 PMID:21356188 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24728327 PMID:25741868 PMID:25927356 PMID:26633542 PMID:27041517 PMID:28492532 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30713837 PMID:31586946 PMID:33558524 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24728327 PMID:25640679 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33558524 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia | ClinVar Annotator: match by term: Fanconi pancytopenia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24728327 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33558524 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia | ClinVar Annotator: match by term: Fanconi's anemia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24728327 PMID:25640679 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:30716324 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33558524 PMID:34585473 PMID:9536098


  • An association has been curated linking Fancd2 and Fanconi anemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FANCD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 83 RGD objects have been annotated to Fanconi anemia  (DOID:13636)
  • 11 papers in RGD have been used to annotate Fancd2
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia | ClinVar Annotator: match by term: Fanconi pancytopenia | ClinVar Annotator: match by term: Fanconi's anemia
  • Original References(s): PMID:11239453 PMID:14695169 PMID:16199547 PMID:16280053 PMID:17096012 PMID:17308347 PMID:17436244 PMID:17576681 PMID:21356188 PMID:22720145 PMID:22828868 PMID:22829014 PMID:23285130 PMID:23613520 PMID:24033266 PMID:24584348 PMID:24728327 PMID:25640679 PMID:25703294 PMID:25741868 PMID:25927356 PMID:26580448 PMID:26633542 PMID:26740942 PMID:27041517 PMID:27153395 PMID:27931139 PMID:28202063 PMID:28386063 PMID:28492532 PMID:28678401 PMID:29625052 PMID:29659569 PMID:30250602 PMID:30256826 PMID:30306255 PMID:30713837 PMID:30716324 PMID:31586946 PMID:32546565 PMID:32659967 PMID:33270637 PMID:33558524 PMID:34327028 PMID:34585473 PMID:9536098


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